A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739770



Internal ID20515746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201563127..201563181hg38UCSC Ensembl
chr2:202427850..202427904hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286299
Samples
Known GenesALS2CR11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739770
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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